Title of article :
Reduced L-selectin (CD62LLow) expression identifies tumor-specific type 1 T cells from lymph nodes draining an autologous tumor cell vaccine
Author/Authors :
Meijer، نويسنده , , Sybren L. and Dols، نويسنده , , Annemieke and Hu، نويسنده , , Hong-Ming and Chu، نويسنده , , Yiwei and Romero، نويسنده , , Pedro and Urba، نويسنده , , Walter J. and Fox، نويسنده , , Bernard A.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2004
Pages :
10
From page :
93
To page :
102
Abstract :
Reduced expression of CD62L can identify tumor-specific T cells in lymph nodes draining murine tumors. Here, we examined whether this strategy could isolate tumor-specific T cells from vaccinated patients. Tumor vaccine-draining lymph node (TVDLN) T cells of seven patients were separated into populations with reduced (CD62LLow) or high levels of CD62L (CD62LHigh). Effector T cells generated from CD62LLow cells maintained or enriched the autologous tumor-specific type 1 cytokine response compared to unseparated TVDLN T cells in four of four patients showing tumor-specific cytokine secretion. Interestingly, effector T cells generated from CD62LLow or CD62LHigh TVDLN were polarized towards a dominant type 1 or type 2 cytokine profile, respectively. For CD62LLow T cells the type 1 cytokine profile appeared determined prior to culture. Since a tumor-specific type 1 cytokine profile appears critical for mediating anti-tumor activity in vivo, this approach might be used to isolate T cells for adoptive immunotherapy.
Keywords :
Sentinel lymph node , IFN-? , Tumor vaccine , IL-5 , Tumor-specific T cells , immunotherapy , melanoma , renal cell carcinoma , tetramer
Journal title :
Cellular Immunology
Serial Year :
2004
Journal title :
Cellular Immunology
Record number :
1856716
Link To Document :
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